Evidence map›Paper›PMID 27232499›Full record

ArticlePloS one2016

A Probabilistic Boolean Network Approach for the Analysis of Cancer-Specific Signalling: A Case Study of Deregulated PDGF Signalling in GIST.

Panuwat Trairatphisan, Monique Wiesinger, Christelle Bahlawane, Serge Haan, Thomas Sauter

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  5. Boolean network modeling in systems pharmacology.Journal of pharmacokinetics and pharmacodynamics · 2018
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Panuwat TrairatphisanSystems Biology group, Life Sciences Research Unit, University of Luxembourg, Luxembourg, Luxembourg.ORCID http://orcid.org/0000-0002-1124-5375
Monique WiesingerSystems Biology group, Life Sciences Research Unit, University of Luxembourg, Luxembourg, Luxembourg.
Christelle BahlawaneMolecular disease mechanisms group, Life Sciences Research Unit, University of Luxembourg, Luxembourg, Luxembourg.
Serge HaanMolecular disease mechanisms group, Life Sciences Research Unit, University of Luxembourg, Luxembourg, Luxembourg.
Thomas SauterSystems Biology group, Life Sciences Research Unit, University of Luxembourg, Luxembourg, Luxembourg.
University of Luxembourg · LU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSignal transduction networks are increasingly studied with mathematical modelling approaches while each of them is suited for a particular problem. For the contextualisation and analysis of signalling networks with steady-state protein data, we identified probabilistic Boolean network (PBN) as a promising framework which could capture quantitative changes of molecular changes at steady-state with a minimal parameterisation. RESULTS AND

conclusionIn our case study, we successfully applied the PBN approach to model and analyse the deregulated Platelet-Derived Growth Factor (PDGF) signalling pathway in Gastrointestinal Stromal Tumour (GIST). We experimentally determined a rich and accurate dataset of steady-state profiles of selected downstream kinases of PDGF-receptor-alpha mutants in combination with inhibitor treatments. Applying the tool optPBN, we fitted a literature-derived candidate network model to the training dataset consisting of single perturbation conditions. Model analysis suggested several important crosstalk interactions. The validity of these predictions was further investigated experimentally pointing to relevant ongoing crosstalk from PI3K to MAPK signalling in tumour cells. The refined model was evaluated with a validation dataset comprising multiple perturbation conditions. The model thereby showed excellent performance allowing to quantitatively predict the combinatorial responses from the individual treatment results in this cancer setting. The established optPBN pipeline is also widely applicable to gain a better understanding of other signalling networks at steady-state in a context-specific fashion.

Indexed as

Signal TransductionComputational BiologyGastrointestinal Stromal TumorsHumansMAP Kinase Signaling SystemPlatelet-Derived Growth FactorPoint MutationProbabilityPlatelet-Derived Growth Factor

Identifiers

PMID27232499
PMCPMC4883749
OpenAlexW2394932368

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.